Autoantibodies and other tests in rheum Flashcards
Scl-70 (anti-topoisomerase)
40% of diffuse scleroderma
15% limited
- higher risk of ILD
RNA polymerase III
17% in scleroderma
- increased risk of renal crisis
- increased risk of malignancy
anti-centromere antibodies
80% of limited scleroderma (CREST)
Anti-Jo-1
Polymyositis
Anti-Synthetase syndrome
Anti-Mi2
Dermatomyositis
Pattern of ANA seen in limited systemic sclerosis?
Centromere
Pattern of ANA seen in diffuse systemic sclerosis?
Speckled
Pattern of ANA seen in poly/dermatomyositis?
Speckled
Pattern of ANA seen in sjogrens?
Speckled
Pattern of ANA seen in lupus?
Homogeneous and rim pattern most specific
Anti-ds DNA
SLE
- highly specific but only 70% sensitive
- only 70% of patients with SLE have positive dsDNA
Anti-histone antibodies
SLE
- often indicate drug induced lupus
ANA pattern in RA
Homogeneous
Most common and least specific ANA pattern
Speckled
What tests are useful for monitoring SLE?
Anti dsDNA
Complement, ESR, renal function, urinalysis for protein
What is considered a high titre ANA?
1:640
Rheumatoid factor?
Rheumatoid arthritis
As sensitive as anti-CCP (around 70%) but less specific
Can be positive in:
Sjogrens
SLE
Hepatitis C, sarcoid, infective endocarditis, cryoglobulinemia
Anti-CCP?
Specific for RA (more specific then RF but same sensitivity)
Predicts more erosive and more severe disease
Anti-Ro/La
Sjogrens syndrome (70% sensitivity)
SLE (30% sensitivity)
- in SLE predicts higher rate of neonatal lupus (rash and complete heart block)
- women with anti-Ro antibody, carry a 3% chance of having a baby with neonatal lupus
cANCA
anti-neutrophil antibody against proteinase-3
Granulomatosis with polyangiitis (90% sensitivity when disease is active, not used for monitoring)
pANCA
anti-neutrophil antibody against myeloperoxidase
microscopic polyangiitis - 80% sensitivity
churg strauss - 60% sensitivity
* note atypical pANCA (not MPO) can be seen in inflammatory bowel disease
Type 1 cryoglobulins
Monoclonal IgM or IgG
- caused by lymphoproliferative disorders Waldenstroms, MM, lymphoma
- not particulary good at activating complement so do not become clinically apparent until high enough to cause hyperviscosity
Type 2 cryoglobulins
Monoclonal RF (usually IgM or IgA) against the Fc portion of IgG
- most associated with hep C and HIV
- most common type
Type 3 cryoglobulins
Polyclonal RF against IgG
- most associated with underlying connective tissue disorders
What is meant by mixed cryoglobulinemia?
Type 2 and 3
- types that involve RF
What is a cryoglobulin?
Immunoglobulins that precipitate in the cold and dissolve on re-warming
Complement levels in mixed cryoglobulinemia?
Low C4 and normal C3
Complement levels in a lupus flare?
Low C3 and C4
- activation of classical pathway = both low
- activation of alternative pathway = low C3 and normal C4
Complement findings in post strep GN?
Low C3 and normal C4